All diseases

OMIM ID
258501
OMIM term:
3-@METHYLGLUTACONIC ACIDURIA, TYPE III; MGCA3
Alternative terms:
MGA, TYPE III; MGA3
OPTIC ATROPHY PLUS SYNDROME
OPTIC ATROPHY, INFANTILE, WITH CHOREA AND SPASTIC PARAPLEGIA
IRAQI-JEWISH 'OPTIC ATROPHY PLUS'
COSTEFF SYNDROME
OPTIC ATROPHY 3, AUTOSOMAL RECESSIVE
OPA3, AUTOSOMAL RECESSIVE
(∗) Location:
19q13.32  
(†) Associated OMIM genes:
OPA3  
(‡) Associated MGI genes:
Opa3  

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